High Dose Re-Irradiation Utilizing Advanced Deformable Image Registration (DIR) and Individualized Organ At Risk (OAR) Dose Calculations With Organ Specific Toxicity Analysis

Official title

High Dose Re-Irradiation Utilizing Advanced Deformable Image Registration (DIR) and Individualized Organ At Risk (OAR) Dose Calculations With Organ Specific Toxicity Analysis (REDIRICT)

Overview

This trial applies a uniform approach to re-irradiation for planning and diagnostic image fusion, dose summation, dose calculations, and follow up for tumor control and detailed toxicity analysis of serial Organs At Risk (OARs). Serial organs include named arteries and nerves, spinal cord, and gastrointestinal tract.

Detailed description

STUDY DESIGN: For each serial OAR, we expect that 10% or less of reirradiated patients will have a Grade 3-5 toxicity. Under this assumption, 15 patients treated at a defined OAR will provide a 90% confidence interval (CI) for the Grade 3-5 OAR toxicity rate with a CI width no larger than 29%. A total of 120 treated patients (15 per OAR) are needed to provide this level of precision for toxicity rates within all 8 OARs (spinal cord, brachial plexus, named vessels, esophagus, duodenum, rectum, proximal bronchus/trachea, liver).

For each OAR, the numbers of patients reirradiated and Grade 3-5 toxicities among them will be tabulated. The Grade 3-5 toxicity rate among treated patients will be estimated separately for each OAR using the sample proportion and a 90% Wilson score confidence interval. Only patients who initiate re-irradiation therapy will be included in this analysis.

Interventions

• Radiation Re-irradiation
  Patients will undergo re-irradiation following treatment planning based on current standard practice as determined by treating physicians and multidisciplinary teams.

Primary outcome measures

• Organ-specific grade 3 toxicity. [Time frame: Up to 24 months]
• Organ-specific grade 4 toxicity. [Time frame: Up to 24 months]
• Organ-specific grade 5 toxicity. [Time frame: Up to 24 months]

Eligibility criteria

Inclusion criteria

• Provision of signed informed consent
• Patients ≥18 years of age receiving definitive or postoperative high dose radiation to volume that includes overlap with previously irradiated OAR(s).
• Prior radiation dosimetry must be available.
• Participants must have stage I-IV biopsy proven solid malignancy (histologic proof or unequivocal cytologic proof solid tumor malignancy from either the primary or any metastatic site). Documentation of pathology reports are required. Local review of pathology or cytology is at the discretion of the multidisciplinary team.
• Histologic confirmation of target lesion recurrence is recommended.
• Documentation of consensus for recommendation of reirradiation by multidisciplinary team and location of target lesion or postoperative site to be treated.
• Documentation of whether or not concurrent cancer therapy drugs are recommended and rationale.
• Documentation of rationale for not obtaining tissue confirmation of the target lesion, if applicable.
• Baseline target lesion imaging with CT, positron emission tomography (PET) /CT, or MRI is required within six weeks of trial enrollment. CT or MRI simulation scans may be used for baseline imaging.
• Patients who have had disease resected in a previously irradiated field and are at high pathological and clinical risk for recurrence as defined by the treating Radiation Oncologist and multidisciplinary team, are eligible for study.
• Measurable disease is not required for patients being treated postoperatively.
• Baseline labs are per standard practice. Values will be dependent on the OARs being treated. (Per standard practice, radiation therapy volumes to OARs are modified to accommodate compromised renal, liver, pulmonary or other OAR function). Recommended labs and values include:

• Aspartate transaminase (AST) and alanine transaminase (ALT) < 2.5 x upper limit of normal (ULN) or < 5 x ULN with metastatic liver disease.
• Total bilirubin < 1.5 x ULN
• Absolute neutrophil count (ANC) > 500 cells/mm\^3
• Platelets > 50,000 cells/mm\^3
• Creatinine < 1.5 x ULN or Creatinine clearance > 45 mL/min if creatinine is > 1.5 x ULN (calculated Creatinine Clearance (CrCl) based on Cockcroft-Gault equation)
• Eastern Cooperative Oncology Group (ECOG) Performance Score 0-2.
• Patients must have resolution of acute toxic effect(s) of most recent cancer therapy to Grade 1 or 2.
• Life expectancy of at least 6 months.
• Female patients of childbearing potential must have negative urine or serum pregnancy test within 7 days prior to start of re-irradiation.
• Ability to complete the self-reported questionnaires (translations will be made available if the patient's primary language is not English).
• Concurrent participation on pharmaceutical, investigator-initiated, National Clinical Trials Network (NCTN), or other multisite clinical trials that include re-irradiation is allowed.

Exclusion criteria

• Patients receiving low dose radiation for symptom management only.
• Patients with evidence of severe or uncontrolled systemic conditions.
• Life expectancy of less than 6 months.
• ECOG Performance status ≥ 3.
• Women of childbearing potential who are known to be pregnant or are unwilling to use an acceptable method of contraception from the time of informed consent until completion of the course of radiotherapy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

United States · 1 center

• Froedtert Hospital — Milwaukee

Identifiers

NCT: NCT05301101 · PRO00042951

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗